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CAS 16355-00-3

(R)-(-)-1-Phenylethane-1,2-diol TCI P1150

(R)-(-)-1-Phenylethane-1,2-diol TCI P1150

Chemical Identity

CAS No.
16355-00-3
PubChem
CID 2724621·SID 87575252
Formula
C8H10O2
Molecular weight
138.16 g/mol
Purity
>98.0%(GC)
Reference databases
ChEBI·ChemSpider·ECHA
Full identifiers (IUPAC, SMILES, InChIKey)
IUPAC
(1R)-1-phenylethane-1,2-diol
SMILES
C1=CC=C(C=C1)[C@H](CO)O
InChIKey
PWMWNFMRSKOCEY-QMMMGPOBSA-N
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(R)-(-)-1-Phenylethane-1,2-diol is a chiral compound widely used in asymmetric synthesis to construct molecules with specific biological activities. This compound plays a key role in the development of chiral structures, which are essential in pharmaceutical and organic chemistry research. Its unique stereochemistry allows for the synthesis of enantiomers with distinct pharmacological effects, making it a valuable tool in the laboratory. The compound's molecular structure features two asymmetric centers, enabling the formation of different enantiomers. This characteristic is crucial for creating compounds with desired optical properties.

The compound is preferred due to its chemical stability under controlled laboratory conditions and its ability to yield optically active products. Its chiral nature ensures that it can be used in the synthesis of complex molecules with precise stereochemical control. The compound's reliability and consistency make it a trusted choice for researchers working on asymmetric synthesis projects. Additionally, its availability and well-defined chemical properties support its use in various synthetic pathways.

In Indonesian laboratories, (R)-(-)-1-Phenylethane-1,2-diol is commonly used by researchers and the pharmaceutical industry for the development of new drugs. Its role in creating chiral compounds is vital for advancing organic chemistry and asymmetric synthesis. The compound is a key component in the research efforts aimed at producing pharmaceuticals with specific therapeutic effects.

TCI brochures (PDF)

  • Asymmetric Synthesis: This compound is ideal for creating enantiomers with distinct pharmacological properties, enabling the development of more effective and targeted pharmaceuticals.
  • Chiral Compound Development: Its stereochemical properties make it a preferred choice for synthesizing chiral molecules with specific biological activities.
  • Organic Chemistry Research: The compound supports the synthesis of complex organic structures, contributing to advancements in chemical research.
  • Pharmaceutical Innovation: It is widely used in the creation of new drug molecules that require precise stereochemical control for optimal therapeutic effects.
  • Structural Analysis Studies: Its well-defined chiral structure aids in the study of molecular interactions and stereochemical behavior in various chemical processes.

Brand TCI
CAS number 16355-00-3
Molecular formula —
Purity —
Category Chemistry > Asymmetric Synthesis > Chiral Building Blocks
Pack sizes Available in various quantities as per standard laboratory supply
Physical form Solid (exact form may vary depending on supplier)
Storage Store in a cool, dry place away from light and moisture

This compound should be stored in a cool, dry environment, away from direct light and moisture to maintain its chemical integrity. It is recommended to use airtight containers to prevent exposure to air and humidity. Proper labeling of storage containers is essential for safe handling and identification. Laboratory personnel should wear appropriate personal protective equipment, such as gloves and safety goggles, when handling the compound. The compound should be kept in a secure location to prevent accidental spills or contamination. Regular monitoring of storage conditions ensures the compound remains stable and suitable for use in research applications.

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